Evidence map›Paper›PMID 38451068›Full record

ArticleDevelopment (Cambridge, England)2024

A multistep computational approach reveals a neuro-mesenchymal cell population in the embryonic hematopoietic stem cell niche.

Olivera Miladinovic, Pierre-Yves Canto, Claire Pouget, Olivier Piau, Nevenka Radic, Priscilla Freschu, Alexandre Megherbi, Carla Brujas Prats, Sebastien Jacques, Estelle Hirsinger and 10 more

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. The evolving hematopoietic niche during development.Frontiers in molecular biosciences · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Olivera MiladinovicLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.
Pierre-Yves CantoLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.
Claire PougetDepartment of Cell and Developmental Biology, University of California San Diego, La Jolla, CA 92093-0380, USA.
Olivier PiauLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.
Nevenka RadicLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.
Priscilla FreschuLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.
Alexandre MegherbiLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.
Carla Brujas PratsLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.
Sebastien JacquesPlateforme de génomique, Université de Paris, Institut Cochin, Inserm, CNRS, F-75014 Paris, France.
Estelle HirsingerLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.ORCID 0000-0002-5256-7741
Audrey GeeverdingService de microscopie électronique, Fr3631 Institut de Biologie Paris Seine, Sorbonne Université, CNRS, 7-9 Quai St-Bernard, 75005 Paris, France.
Sylvie DufourUniversité Paris-Est Créteil, Inserm, IMRB, F94010 Créteil, France.
Laurence PetitLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.
Michele SouyriUniversité de Paris, Inserm UMR 1131, Institut de Recherche Saint Louis, Hôpital Saint Louis, 1 Avenue Claude Vellefaux, 75010 Paris, France.
Trista NorthStem Cell Program, Department of Hematology/Oncology, Boston Children's Hospital, Boston, MA 02115, USA.
Hervé IsambertInstitut Curie, PSL Research University, CNRS UMR168, Paris, France.
David TraverDepartment of Cell and Developmental Biology, University of California San Diego, La Jolla, CA 92093-0380, USA.
Thierry JaffredoLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.ORCID 0000-0002-8724-3261
Pierre CharbordLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.ORCID 0000-0002-2254-3300
Charles DurandLaboratoire de Biologie du Développement/UMR7622, Institut de Biologie Paris Seine, Sorbonne Université, CNRS, Inserm U1156, 9 Quai St-Bernard, 75005 Paris, France.ORCID 0000-0002-1970-0467

Funding

Molecular Circuits in the Hematopoietic Stem Cell NicheRC2DK120535 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI COLLINS, JAMES J, DALEY, GEORGE Q · 2020 to 2024
$8.2M
Molecular and functional dissection of zebrafish hematopoietic stem cell nicheR01DK074482 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TRAVER, DAVID · 2006 to 2024
$6.5M
Developmental Activation of the Inflammasome Controls Hematopoietic Stem Cell ProductionR01HL154580 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI NORTH, TRISTA E. · 2020 to 2023
$2.2M
NHLBI NIH HHS R01 HL154580NIDDK NIH HHS R01 DK074482NIDDK NIH HHS RC2 DK120535NIH HHS NIH DK074482
6 · The paper itself

Abstract

The first hematopoietic stem and progenitor cells (HSPCs) emerge in the Aorta-Gonad-Mesonephros (AGM) region of the mid-gestation mouse embryo. However, the precise nature of their supportive mesenchymal microenvironment remains largely unexplored. Here, we profiled transcriptomes of laser micro-dissected aortic tissues at three developmental stages and individual AGM cells. Computational analyses allowed the identification of several cell subpopulations within the E11.5 AGM mesenchyme, with the presence of a yet unidentified subpopulation characterized by the dual expression of genes implicated in adhesive or neuronal functions. We confirmed the identity of this cell subset as a neuro-mesenchymal population, through morphological and lineage tracing assays. Loss of function in the zebrafish confirmed that Decorin, a characteristic extracellular matrix component of the neuro-mesenchyme, is essential for HSPC development. We further demonstrated that this cell population is not merely derived from the neural crest, and hence, is a bona fide novel subpopulation of the AGM mesenchyme.

Indexed as

Mesenchymal Stem CellsZebrafishAnimalsEmbryo, MammalianGonadsHematopoiesisHematopoietic Stem CellsMesonephrosMiceAorta-Gonad-MesonephrosGene networksHematopoietic stem cellsLaser microdissectionMesenchymeNiche

Identifiers

PMID38451068
PMCPMC11057820

What OpenQuestion holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.